Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | View in dbSNP

Alleles
A/- | Ancestral: A
Location

Chromosome 20:53566987 (forward strand) | View in location tab

Co-located

with dbSNP rs74838016 (A/C)

Most severe consequence
Evidence status

This variation has 2 HGVS names - click the plus to show

Variation displays